# K092503: Radar Vascular Compression Devices

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Vascular Dynamics
- Decided: Nov 19, 2009 after 97 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K984177 (1998). 6 ancestors in all.
9 later devices descend from it; 3 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070423: TR Band, Terumo Medical Corp. (2007) Summary page 1.
- K040208: Neptune Pad, Neptune Disc, Neptune Comfort-Band, Comfort-Band, Tz Medical, Inc. (2004) Summary page 1.

## Most influential descendants
- K111837: Radial Artery Compression Tourniquet (2011), 4 descendants of its own
- K142122: Radar Vascular Compression Device (2014), 3 descendants of its own
- K142359: Vasc Band hemostat (2014), 3 descendants of its own
- K162988: PreludeSYNC Radial Compression Device (2017), 1 descendant of its own
- K151363: Zephyr Vascular Compression Device (2015), 1 descendant of its own

## Indications for use
The RADAR Vascular Compression Devices are indicated for use by medical professionals to promote hemostasis following a catheterization or other puncture into a blood vessel in a patient's arm, including radial artery catheterization, arterial or venous line removal, hemodialysis, and in patients on anticoagulation therapy.

Source page: https://510kreport.com/device/K092503
Methodology: https://510kreport.com/methodology